![Hsp60 (HSPD1) Mouse Monoclonal Antibody [Clone ID: LBI1B3]](https://img1.dxycdn.com/2022/0707/344/1496323853485278553-14.jpg)
- ￥3300
- Leading Biology
- AMM14801VCF
- 美国
- 2025年07月14日
- WB 1:500, IHC 1:150
- Mouse
- Human, Mouse, Rat
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- 详细信息
- 技术资料
- 靶点：
HSPD1
- 应用范围：
WB 1:500, IHC 1:150
- 宿主：
Mouse
- 适应物种：
Human, Mouse, Rat
- 保质期：
1-2年
- 供应商：
安诺伦（北京）生物科技有限公司
- 标记物：
Unconjugated
- 克隆性：
Monoclonal Antibody
- 保存条件：
Stable for 1 year at -20°C from date of shipment. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.
- 形态：
Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)
- 亚型：
IgG1
- 免疫原：
Full length human recombinant protein of human HSPD1 (NP_955472) produced in E.coli.
- 规格：
100 ug
别名：CPN60; GROEL; HLD4; HSP-60; HSP60; HSP65; HuCHA60; SPG13
产品概述：Carrier-free (BSA/glycerol-free) HSPD1 mouse monoclonal antibody, clone LBI1B3
总结：This gene encodes a member of the chaperonin family. The encoded mitochondrial protein may function as a signaling molecule in the innate immune system. This protein is essential for the folding and assembly of newly imported proteins in the mitochondria. This gene is adjacent to a related family member and the region between the 2 genes functions as a bidirectional promoter. Several pseudogenes have been associated with this gene. Two transcript variants encoding the same protein have been identified for this gene. Mutations associated with this gene cause autosomal recessive spastic paraplegia 13. [provided by RefSeq, Jun
产品概述：Carrier-free (BSA/glycerol-free) HSPD1 mouse monoclonal antibody, clone LBI1B3
总结：This gene encodes a member of the chaperonin family. The encoded mitochondrial protein may function as a signaling molecule in the innate immune system. This protein is essential for the folding and assembly of newly imported proteins in the mitochondria. This gene is adjacent to a related family member and the region between the 2 genes functions as a bidirectional promoter. Several pseudogenes have been associated with this gene. Two transcript variants encoding the same protein have been identified for this gene. Mutations associated with this gene cause autosomal recessive spastic paraplegia 13. [provided by RefSeq, Jun
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Hsp60 (HSPD1) Mouse Monoclonal Antibody [Clone ID: LBI1B3]
￥3300
